NDC 79260-487 Aris Foaming Handsoap
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What is NDC 79260-487?
What are the uses for Aris Foaming Handsoap?
Which are Aris Foaming Handsoap UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Aris Foaming Handsoap Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)
What is the NDC to RxNorm Crosswalk for Aris Foaming Handsoap?
- RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
- RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".